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rs587779087

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779087(A;A)
Make rs587779087(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47463022
GeneMSH2
is asnp
is mentioned by
dbSNPrs587779087
ebirs587779087
HLIrs587779087
Exacrs587779087
Varsomers587779087
Maprs587779087
PheGenIrs587779087
hapmaprs587779087
1000 genomesrs587779087
hgdprs587779087
ensemblrs587779087
gopubmedrs587779087
geneviewrs587779087
scholarrs587779087
googlers587779087
pharmgkbrs587779087
gwascentralrs587779087
openSNPrs587779087
23andMers587779087
23andMe allrs587779087
SNP Nexus

SNPshotrs587779087
SNPdbers587779087
MSV3drs587779087
GWAS Ctlgrs587779087
Max Magnitude0
ClinVar
Risk rs587779087(A;A)
Alt rs587779087(A;A)
Reference rs587779087(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH2
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.47690161T>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000076144.2,